연구자에게
내 논문이 여기 있나요?
논문 2,665편이 이 사이트를 떠받치고 있습니다. 모든 변이·질환 페이지가
자기가 어떤 연구로부터 쓰였는지 밝히며, 이것이 그 목록을 페이지들에서 모은 것입니다.
성함이나 학술지명, PMID로 찾아보십시오.
23andMe Research team에 대해
70건, 그중 20건 표시.
Multi-trait analysis of genome-wide association summary statistics using MTAG
Turley P,
Walters RK,
Maghzian O,
Okbay A,
Lee JJ,
Fontana MA,
Nguyen-Viet TA,
Wedow R,
Zacher M,
Furlotte NA,
Magnusson P,
Oskarsson S
외 6명 — 모두 보기
23andMe Research Team · Social Science Genetic Association Consortium
Nature genetics · 2018 · PMID 29292387 · open access
페이지 12개+
Genome-wide association study of depression phenotypes in UK Biobank identifies variants in excitatory synaptic pathways
Howard DM,
Adams MJ,
Shirali M,
Clarke TK,
Marioni RE,
Davies G,
Coleman JRI,
Alloza C,
Shen X,
Barbu MC,
Wigmore EM,
Gibson J
외 9명 — 모두 보기
23andMe Research Team
Nature communications · 2018 · PMID 29662059 · open access
페이지 12개+
Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error
Tedja MS,
Wojciechowski R,
Hysi PG,
Eriksson N,
Furlotte NA,
Verhoeven VJM,
Iglesias AI,
Meester-Smoor MA,
Tompson SW,
Fan Q,
Khawaja AP,
Cheng CY
외 86명 — 모두 보기
Höhn R,
Yamashiro K,
Wenocur A,
Grazal C,
Haller T,
Metspalu A,
Wedenoja J,
Jonas JB,
Wang YX,
Xie J,
Mitchell P,
Foster PJ,
Klein BEK,
Klein R,
Paterson AD,
Hosseini SM,
Shah RL,
Williams C,
Teo YY,
Tham YC,
Gupta P,
Zhao W,
Shi Y,
Saw WY,
Tai ES,
Sim XL,
Huffman JE,
Polašek O,
Hayward C,
Bencic G,
Rudan I,
Wilson JF,
Joshi PK,
Tsujikawa A,
Matsuda F,
Whisenhunt KN,
Zeller T,
van der Spek PJ,
Haak R,
Meijers-Heijboer H,
van Leeuwen EM,
Iyengar SK,
Lass JH,
Hofman A,
Rivadeneira F,
Uitterlinden AG,
Vingerling JR,
Lehtimäki T,
Raitakari OT,
Biino G,
Concas MP,
Schwantes-An TH,
Igo RP Jr,
Cuellar-Partida G,
Martin NG,
Craig JE,
Gharahkhani P,
Williams KM,
Nag A,
Rahi JS,
Cumberland PM,
Delcourt C,
Bellenguez C,
Ried JS,
Bergen AA,
Meitinger T,
Gieger C,
Wong TY,
Hewitt AW,
Mackey DA,
Simpson CL,
Pfeiffer N,
Pärssinen O,
Baird PN,
Vitart V,
Amin N,
van Duijn CM,
Bailey-Wilson JE,
Young TL,
Saw SM,
Stambolian D,
MacGregor S,
Guggenheim JA,
Tung JY,
Hammond CJ,
Klaver CCW
CREAM Consortium · 23andMe Research Team 외 컨소시엄 1곳
Nature genetics · 2018 · PMID 29808027 · open access
페이지 12개+
Meta-analysis of genome-wide association studies for neuroticism in 449,484 individuals identifies novel genetic loci and pathways
Nagel M,
Jansen PR,
Stringer S,
Watanabe K,
de Leeuw CA,
Bryois J,
Savage JE,
Hammerschlag AR,
Skene NG,
Muñoz-Manchado AB,
White T,
Tiemeier H
외 6명 — 모두 보기
23andMe Research Team
Nature genetics · 2018 · PMID 29942085
페이지 12개+
Genome-wide association and HLA fine-mapping studies identify risk loci and genetic pathways underlying allergic rhinitis
Waage J,
Standl M,
Curtin JA,
Jessen LE,
Thorsen J,
Tian C,
Schoettler N,
Flores C,
Abdellaoui A,
Ahluwalia TS,
Alves AC,
Amaral AFS
외 76명 — 모두 보기
Antó JM,
Arnold A,
Barreto-Luis A,
Baurecht H,
van Beijsterveldt CEM,
Bleecker ER,
Bonàs-Guarch S,
Boomsma DI,
Brix S,
Bunyavanich S,
Burchard EG,
Chen Z,
Curjuric I,
Custovic A,
den Dekker HT,
Dharmage SC,
Dmitrieva J,
Duijts L,
Ege MJ,
Gauderman WJ,
Georges M,
Gieger C,
Gilliland F,
Granell R,
Gui H,
Hansen T,
Heinrich J,
Henderson J,
Hernandez-Pacheco N,
Holt P,
Imboden M,
Jaddoe VWV,
Jarvelin MR,
Jarvis DL,
Jensen KK,
Jónsdóttir I,
Kabesch M,
Kaprio J,
Kumar A,
Lee YA,
Levin AM,
Li X,
Lorenzo-Diaz F,
Melén E,
Mercader JM,
Meyers DA,
Myers R,
Nicolae DL,
Nohr EA,
Palviainen T,
Paternoster L,
Pennell CE,
Pershagen G,
Pino-Yanes M,
Probst-Hensch NM,
Rüschendorf F,
Simpson A,
Stefansson K,
Sunyer J,
Sveinbjornsson G,
Thiering E,
Thompson PJ,
Torrent M,
Torrents D,
Tung JY,
Wang CA,
Weidinger S,
Weiss S,
Willemsen G,
Williams LK,
Ober C,
Hinds DA,
Ferreira MA,
Bisgaard H,
Strachan DP,
Bønnelykke K
23andMe Research Team · AAGC collaborators
Nature genetics · 2018 · PMID 30013184
페이지 12개+
Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals
Lee JJ,
Wedow R,
Okbay A,
Kong E,
Maghzian O,
Zacher M,
Nguyen-Viet TA,
Bowers P,
Sidorenko J,
Karlsson Linnér R,
Fontana MA,
Kundu T
외 65명 — 모두 보기
Lee C,
Li H,
Li R,
Royer R,
Timshel PN,
Walters RK,
Willoughby EA,
Yengo L,
Alver M,
Bao Y,
Clark DW,
Day FR,
Furlotte NA,
Joshi PK,
Kemper KE,
Kleinman A,
Langenberg C,
Mägi R,
Trampush JW,
Verma SS,
Wu Y,
Lam M,
Zhao JH,
Zheng Z,
Boardman JD,
Campbell H,
Freese J,
Harris KM,
Hayward C,
Herd P,
Kumari M,
Lencz T,
Luan J,
Malhotra AK,
Metspalu A,
Milani L,
Ong KK,
Perry JRB,
Porteous DJ,
Ritchie MD,
Smart MC,
Smith BH,
Tung JY,
Wareham NJ,
Wilson JF,
Beauchamp JP,
Conley DC,
Esko T,
Lehrer SF,
Magnusson PKE,
Oskarsson S,
Pers TH,
Robinson MR,
Thom K,
Watson C,
Chabris CF,
Meyer MN,
Laibson DI,
Yang J,
Johannesson M,
Koellinger PD,
Turley P,
Visscher PM,
Benjamin DJ,
Cesarini D
23andMe Research Team · COGENT (Cognitive Genomics Consortium) 외 컨소시엄 1곳
Nature genetics · 2018 · PMID 30038396
페이지 12개+
An atlas of genetic influences on osteoporosis in humans and mice
Morris JA,
Kemp JP,
Youlten SE,
Laurent L,
Logan JG,
Chai RC,
Vulpescu NA,
Forgetta V,
Kleinman A,
Mohanty ST,
Sergio CM,
Quinn J
외 47명 — 모두 보기
Nguyen-Yamamoto L,
Luco AL,
Vijay J,
Simon MM,
Pramatarova A,
Medina-Gomez C,
Trajanoska K,
Ghirardello EJ,
Butterfield NC,
Curry KF,
Leitch VD,
Sparkes PC,
Adoum AT,
Mannan NS,
Komla-Ebri DSK,
Pollard AS,
Dewhurst HF,
Hassall TAD,
Beltejar MG,
Adams DJ,
Vaillancourt SM,
Kaptoge S,
Baldock P,
Cooper C,
Reeve J,
Ntzani EE,
Evangelou E,
Ohlsson C,
Karasik D,
Rivadeneira F,
Kiel DP,
Tobias JH,
Gregson CL,
Harvey NC,
Grundberg E,
Goltzman D,
Adams DJ,
Lelliott CJ,
Hinds DA,
Ackert-Bicknell CL,
Hsu YH,
Maurano MT,
Croucher PI,
Williams GR,
Bassett JHD,
Evans DM,
Richards JB
23andMe Research Team
Nature genetics · 2019 · PMID 30598549 · open access
페이지 12개+
Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use
Liu M,
Jiang Y,
Wedow R,
Li Y,
Brazel DM,
Chen F,
Datta G,
Davila-Velderrain J,
McGuire D,
Tian C,
Zhan X,
Choquet H
외 111명 — 모두 보기
Docherty AR,
Faul JD,
Foerster JR,
Fritsche LG,
Gabrielsen ME,
Gordon SD,
Haessler J,
Hottenga JJ,
Huang H,
Jang SK,
Jansen PR,
Ling Y,
Mägi R,
Matoba N,
McMahon G,
Mulas A,
Orrù V,
Palviainen T,
Pandit A,
Reginsson GW,
Skogholt AH,
Smith JA,
Taylor AE,
Turman C,
Willemsen G,
Young H,
Young KA,
Zajac GJM,
Zhao W,
Zhou W,
Bjornsdottir G,
Boardman JD,
Boehnke M,
Boomsma DI,
Chen C,
Cucca F,
Davies GE,
Eaton CB,
Ehringer MA,
Esko T,
Fiorillo E,
Gillespie NA,
Gudbjartsson DF,
Haller T,
Harris KM,
Heath AC,
Hewitt JK,
Hickie IB,
Hokanson JE,
Hopfer CJ,
Hunter DJ,
Iacono WG,
Johnson EO,
Kamatani Y,
Kardia SLR,
Keller MC,
Kellis M,
Kooperberg C,
Kraft P,
Krauter KS,
Laakso M,
Lind PA,
Loukola A,
Lutz SM,
Madden PAF,
Martin NG,
McGue M,
McQueen MB,
Medland SE,
Metspalu A,
Mohlke KL,
Nielsen JB,
Okada Y,
Peters U,
Polderman TJC,
Posthuma D,
Reiner AP,
Rice JP,
Rimm E,
Rose RJ,
Runarsdottir V,
Stallings MC,
Stančáková A,
Stefansson H,
Thai KK,
Tindle HA,
Tyrfingsson T,
Wall TL,
Weir DR,
Weisner C,
Whitfield JB,
Winsvold BS,
Yin J,
Zuccolo L,
Bierut LJ,
Hveem K,
Lee JJ,
Munafò MR,
Saccone NL,
Willer CJ,
Cornelis MC,
David SP,
Hinds DA,
Jorgenson E,
Kaprio J,
Stitzel JA,
Stefansson K,
Thorgeirsson TE,
Abecasis G,
Liu DJ,
Vrieze S
23andMe Research Team · HUNT All-In Psychiatry
Nature genetics · 2019 · PMID 30643251 · open access
페이지 12개+
Genome-wide meta-analysis of depression identifies 102 independent variants and highlights the importance of the prefrontal brain regions
Howard DM,
Adams MJ,
Clarke TK,
Hafferty JD,
Gibson J,
Shirali M,
Coleman JRI,
Hagenaars SP,
Ward J,
Wigmore EM,
Alloza C,
Shen X
외 26명 — 모두 보기
Barbu MC,
Xu EY,
Whalley HC,
Marioni RE,
Porteous DJ,
Davies G,
Deary IJ,
Hemani G,
Berger K,
Teismann H,
Rawal R,
Arolt V,
Baune BT,
Dannlowski U,
Domschke K,
Tian C,
Hinds DA,
Trzaskowski M,
Byrne EM,
Ripke S,
Smith DJ,
Sullivan PF,
Wray NR,
Breen G,
Lewis CM,
McIntosh AM
23andMe Research Team · Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium
Nature neuroscience · 2019 · PMID 30718901
페이지 12개+
Genome-wide analysis of insomnia in 1,331,010 individuals identifies new risk loci and functional pathways
Jansen PR,
Watanabe K,
Stringer S,
Skene N,
Bryois J,
Hammerschlag AR,
de Leeuw CA,
Benjamins JS,
Muñoz-Manchado AB,
Nagel M,
Savage JE,
Tiemeier H
외 12명 — 모두 보기
White T,
Tung JY,
Hinds DA,
Vacic V,
Wang X,
Sullivan PF,
van der Sluis S,
Polderman TJC,
Smit AB,
Hjerling-Leffler J,
Van Someren EJW,
Posthuma D
23andMe Research Team
Nature genetics · 2019 · PMID 30804565
페이지 12개+
Genome wide analysis for mouth ulcers identifies associations at immune regulatory loci
Dudding T,
Haworth S,
Lind PA,
Sathirapongsasuti JF,
Tung JY,
Mitchell R,
Colodro-Conde L,
Medland SE,
Gordon S,
Elsworth B,
Paternoster L,
Franks PW
외 3명 — 모두 보기
23andMe Research Team
Nature communications · 2019 · PMID 30837455 · open access
페이지 12개+
Genetic Architectures of Childhood- and Adult-Onset Asthma Are Partly Distinct
Ferreira MAR,
Mathur R,
Vonk JM,
Szwajda A,
Brumpton B,
Granell R,
Brew BK,
Ullemar V,
Lu Y,
Jiang Y,
Magnusson PKE,
Karlsson R
외 4명 — 모두 보기
23andMe Research Team · eQTLGen Consortium 외 컨소시엄 1곳
American journal of human genetics · 2019 · PMID 30929738
페이지 12개+
Combined analysis of keratinocyte cancers identifies novel genome-wide loci
Liyanage UE,
Law MH,
Han X,
An J,
Ong JS,
Gharahkhani P,
Gordon S,
Neale RE,
Olsen CM,
MacGregor S,
Whiteman DC
23andMe Research Team
Human molecular genetics · 2019 · PMID 31174203 · open access
페이지 12개+
Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis
Gallagher CS,
Mäkinen N,
Harris HR,
Rahmioglu N,
Uimari O,
Cook JP,
Shigesi N,
Ferreira T,
Velez-Edwards DR,
Edwards TL,
Mortlock S,
Ruhioglu Z
외 24명 — 모두 보기
Day F,
Becker CM,
Karhunen V,
Martikainen H,
Järvelin MR,
Cantor RM,
Ridker PM,
Terry KL,
Buring JE,
Gordon SD,
Medland SE,
Montgomery GW,
Nyholt DR,
Hinds DA,
Tung JY,
Perry JRB,
Lind PA,
Painter JN,
Martin NG,
Morris AP,
Chasman DI,
Missmer SA,
Zondervan KT,
Morton CC
23andMe Research Team
Nature communications · 2019 · PMID 31649266 · open access
페이지 12개+
Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies
Nalls MA,
Blauwendraat C,
Vallerga CL,
Heilbron K,
Bandres-Ciga S,
Chang D,
Tan M,
Kia DA,
Noyce AJ,
Xue A,
Bras J,
Young E
외 39명 — 모두 보기
von Coelln R,
Simón-Sánchez J,
Schulte C,
Sharma M,
Krohn L,
Pihlstrøm L,
Siitonen A,
Iwaki H,
Leonard H,
Faghri F,
Gibbs JR,
Hernandez DG,
Scholz SW,
Botia JA,
Martinez M,
Corvol JC,
Lesage S,
Jankovic J,
Shulman LM,
Sutherland M,
Tienari P,
Majamaa K,
Toft M,
Andreassen OA,
Bangale T,
Brice A,
Yang J,
Gan-Or Z,
Gasser T,
Heutink P,
Shulman JM,
Wood NW,
Hinds DA,
Hardy JA,
Morris HR,
Gratten J,
Visscher PM,
Graham RR,
Singleton AB
23andMe Research Team · System Genomics of Parkinson's Disease Consortium 외 컨소시엄 1곳
The Lancet. Neurology · 2019 · PMID 31701892
페이지 12개+
Genomic analysis of male puberty timing highlights shared genetic basis with hair colour and lifespan
Hollis B,
Day FR,
Busch AS,
Thompson DJ,
Soares ALG,
Timmers PRHJ,
Kwong A,
Easton DF,
Joshi PK,
Timpson NJ,
Ong KK,
Perry JRB
PRACTICAL Consortium · 23andMe Research Team
Nature communications · 2020 · PMID 32210231 · open access
페이지 12개+
Genetic determinants of daytime napping and effects on cardiometabolic health
Dashti HS,
Daghlas I,
Lane JM,
Huang Y,
Udler MS,
Wang H,
Ollila HM,
Jones SE,
Kim J,
Wood AR,
Weedon MN,
Aslibekyan S
외 2명 — 모두 보기
23andMe Research Team
Nature communications · 2021 · PMID 33568662 · open access
페이지 12개+
Symptom-level modelling unravels the shared genetic architecture of anxiety and depression
Thorp JG,
Campos AI,
Grotzinger AD,
Gerring ZF,
An J,
Ong JS,
Wang W,
Shringarpure S,
Byrne EM,
MacGregor S,
Martin NG,
Medland SE
외 2명 — 모두 보기
23andMe Research Team
Nature human behaviour · 2021 · PMID 33859377
페이지 12개+
Genetic analyses identify widespread sex-differential participation bias
Pirastu N,
Cordioli M,
Nandakumar P,
Mignogna G,
Abdellaoui A,
Hollis B,
Kanai M,
Rajagopal VM,
Parolo PDB,
Baya N,
Carey CE,
Karjalainen J
외 17명 — 모두 보기
Als TD,
Van der Zee MD,
Day FR,
Ong KK,
Morisaki T,
de Geus E,
Bellocco R,
Okada Y,
Børglum AD,
Joshi P,
Auton A,
Hinds D,
Neale BM,
Walters RK,
Nivard MG,
Perry JRB,
Ganna A
FinnGen Study · 23andMe Research Team 외 컨소시엄 1곳
Nature genetics · 2021 · PMID 33888908
페이지 12개+
A large multiethnic GWAS meta-analysis of cataract identifies new risk loci and sex-specific effects
Choquet H,
Melles RB,
Anand D,
Yin J,
Cuellar-Partida G,
Wang W,
Hoffmann TJ,
Nair KS,
Hysi PG,
Lachke SA,
Jorgenson E
23andMe Research Team
Nature communications · 2021 · PMID 34127677 · open access
페이지 12개+
이 목록에 대한 질문
제 논문이 왜 여기 있습니까? 허락한 적이 없습니다.
논문의 내용은 여기에 전혀 옮겨져 있지 않습니다. 이 페이지가 기록하는 것은 MyGeneLog™의
어떤 페이지가 귀하의 연구를 인용하고 있다는 사실과 PubMed의 원문 링크뿐이며, 그것이 곧
인용입니다. 제목과 저자 목록은 도서관 목록이 쓰는 것과 같은 공개 기록인 Europe PMC에서
가져옵니다.
왜 "외 몇 명"이 아니라 저자를 다 적습니까?
622명이 필요했던 연구는 4명이 한 연구와 다른 종류의 연구인데, "et al."은 그것을 지우기
때문입니다. 12명을 먼저 보여 주고 나머지는 한 번 눌러 펼칩니다. 검색은 전원을 대상으로
합니다. 컨소시엄 논문의 187번째 이름도 실재하는 사람이고, 그 사람이 자기 이름을 찾고 있을
수 있습니다.
제 이름이 틀렸거나 논문 정보가 잘못되었습니다.
알려 주시면 고칩니다. 이름은 공개 기록에서 가져오는데 데이터베이스마다 이니셜 표기가
다르고, 같은 형태의 이름을 쓰는 두 사람을 저희가 구분할 수 없는 경우도 있습니다. 추측하기
보다 지적을 받는 편이 낫습니다.
제 논문이 없습니다. 탈락시킨 것입니까?
아닙니다. 이 카탈로그는 작은 팀이 읽을 수 있었던 것으로 모은 것이고, 유럽계 조상 코호트
바깥이 가장 얇습니다. 논문이 없는 것은 아직 아무도 거기까지 가지 못했기 때문이지 검토해서
제외한 것이 아닙니다.
어떤 페이지가 그 논문 위에 서 있는지 볼 수 있습니까?
각 줄에 최대 여섯 개까지 표시되며 각각 링크되어 있습니다. 줄 옆의 숫자는 그 논문을
인용하는 페이지가 모두 몇 개인지입니다.
얼마나 자주 갱신됩니까?
페이지들에서 매시간 다시 만들어집니다. 어떤 페이지가 그 논문 위에 서기 시작하면 그
순간 나타나고 그만두면 사라집니다. 따로 관리하는 목록이 없기 때문인데, 인용은 그 주장을
하는 페이지에 붙어 있어야 하기 때문입니다.